RecruitingNot Applicable

Transfusion Surveillance in Anaesthesia

Belgium50,000 participantsStarted 2022-09-01

Plain-language summary

the aim of this register is to collect exhaustively the different data available surrounding a transfusion act in the context of an active haemorrhage. The aim is to allow different modelling and analysis related to emergency transfusion.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * all patients who have received an hemostasis product Exclusion Criteria: * patient who refused to consent to data analysis and study participation

What they're measuring

Hemostatic evolution through transfusion event

Timeframe: 12 hours

ROTEM measures evolution through transfusion event

Timeframe: 12 hours

Haematologic measures evolution through transfusion event

Timeframe: 12 hours

ionic measures evolution through transfusion event

Timeframe: 12 hours

Trial details

NCT IDNCT06403163

SponsorErasme University Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2030-12-31

View on ClinicalTrials.gov More Transfusion Reaction trials